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Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) ELISA Kits

CYP11B1 encodes a member of the cytochrome P450 superfamily of enzymes. Additionally we are shipping CYP11B1 Antibodies (47) and CYP11B1 Proteins (8) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
CYP11B1 1584 P15538
CYP11B1 110115  
CYP11B1 500892  
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Top CYP11B1 ELISA Kits at antibodies-online.com

Showing 7 out of 15 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Mouse 0.064 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
$757.89
Details
Rat 0.29 ng/mL 0.78-50 ng/mL 96 Tests Log in to see 9 to 11 Days
$800.00
Details
Human 5.8 pg/ml 23.5-1500 pg/mL   96 Tests Log in to see 11 to 13 Days
$910.56
Details
Dog
  96 Tests Log in to see 16 to 21 Days
$999.43
Details
Guinea Pig
  96 Tests Log in to see 16 to 21 Days
$999.43
Details
Monkey
  96 Tests Log in to see 16 to 21 Days
$999.43
Details
Rabbit
  96 Tests Log in to see 16 to 21 Days
$999.43
Details

More ELISA Kits for CYP11B1 Interaction Partners

Human Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) interaction partners

  1. Congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene.

  2. Chimeric CYP11B2 (show CYP11B2 ELISA Kits)/CYP11B1 causing 11beta-hydroxylase deficiency in Chinese patients with congenital adrenal hyperplasia

  3. Seven novel CYP11B1 mutations identified in Chinese patients with 11 beta-hydroxylase deficiency.

  4. Mutations in the CYP11B1 gene are the cause of 11beta-hydroxylase deficiency.

  5. study of the functional consequences of 3 novel and 1 previously described CYP11B1 gene mutations (p.(Arg143Trp), p.(Ala306Val), p.(Glu310Lys) and p.(Arg332Gln)) detected in patients suffering from classical and non-classical 11beta-OHD

  6. Heterogenous immunolocalization of CYP11B2 (show CYP11B2 ELISA Kits) and diffuse immunoreactivity of CYP11B1 were detected.

  7. Data from recombinant proteins suggest three additional mutations in CYP11B1 (p.His125Thrfs*8; p.Leu463_Leu464dup; p.Ser150Leu) can account for congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (classical/non-classical phenotype).

  8. Analysis of the CYP11B1 gene revealed two novel mutations, a small insertion in exon 7 (InsAG393) and a small deletion in exon 2 (DelG766), and three previously known missense mutations (T318M, Q356X, and R427H).

  9. Expression of P45011beta and StAR (steroidogenic acute regulatory protein (show STAR ELISA Kits)) is down-regulated in adrenocortical cells and neurons under oxidative stress by ALADIN (show AAAS ELISA Kits) (triple A syndrome protein, human) knockdown.

  10. Identification and functional characterization of a large deletion of the CYP11B1 gene causing an 11beta-Hydroxylase deficiency.

Mouse (Murine) Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) interaction partners

  1. Cyp11b1 is induced in the murine gonad by luteinizing hormone/human chorionic gonadotropin and involved in the production of 11-ketotestosterone, a major fish androgen.

  2. 3-methylsulfonyl-DDE and related compounds did not alter Cyp11b1 gene expression in adrenocortical Y-1 cells indicating that compound-induced enzyme inhibition occurs on the protein level.

  3. These data showed that in the adrenal gland, PREB (show PREB ELISA Kits) regulates the transcription of the CYP11B1 gene via cAMP.

  4. Cyp11b1 null mouse, a model of congenital adrenal hyperplasia

Cow (Bovine) Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) interaction partners

  1. A simultaneous analysis of the influence of CYP11B1 and DGAT1 (show DGAT1 ELISA Kits) on multiple variables of a German Holstein pedigree is presented.

CYP11B1 Antigen Profile

Antigen Summary

This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane and is involved in the conversion of progesterone to cortisol in the adrenal cortex. Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency. Transcript variants encoding different isoforms have been noted for this gene.

Gene names and symbols associated with CYP11B1

  • cytochrome P450, family 11, subfamily B, polypeptide 1 (CYP11B1) antibody
  • cytochrome P450, family 11, subfamily b, polypeptide 1 (Cyp11b1) antibody
  • cytochrome P450, subfamily XI B, polypeptide 1 (CYP11B1) antibody
  • AA389061 antibody
  • Cp11ba antibody
  • CPN1 antibody
  • Cyp11b antibody
  • Cyp11b-1 antibody
  • FHI antibody
  • P450c11 antibody
  • RATCP11BA antibody

Protein level used designations for CYP11B1

cytochrome P450 11B1, mitochondrial , CYPXIB1 , cytochrome P-450c11 , cytochrome P450, subfamily XIB (steroid 11-beta-hydroxylase), polypeptide 1 , cytochrome P450C11 , cytochrome p450 XIB1 , steroid 11-beta-hydroxylase , steroid 11-beta-monooxygenase , steroid-11-beta-hydroxylase , Cytochrome P450, subfamily XIB, polypeptide 1 (steroid 11-beta-hydroxylase) , P450(11 beta)-DS , P450C11 , aldosterone synthase , cytochrome P450(11 beta)-DS , cytochrome P450, subfamily 11B, polypeptide 1 , 11-beta-hydroxylase , 11beta-hydroxylase

GENE ID SPECIES
695793 Macaca mulatta
1584 Homo sapiens
110115 Mus musculus
500892 Rattus norvegicus
100135511 Cavia porcellus
767576 Ovis aries
282422 Bos taurus
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